Subscribe to RSS
DOI: 10.1055/s-0041-1731011
Paraganglioma of the Cauda Equina – Case Report and Literature Review
Paraganglioma de cauda equina – Relato de caso e revisão da LiteraturaAbstract
Paragangliomas of the cauda equina are tumors of rare incidence, with ~ 220 cases described in the world literature. They are benign lesions, grade I by the World Health Organization (WHO), whose definitive diagnosis can only be made by immunohistochemical analysis. Its neuroendocrine nature is evidenced by the presence of chromogranin. The relevance of reporting this case is because paragangliomas of the cauda equina should be included among the differential diagnoses of intradural and extramedullary tumors, and especially because they can cause perioperative and intraoperative hypertensive crises by adrenergic discharge.
The present study presents the case of a 36-year-old male patient diagnosed with a lumbar spine tumor located in the central spinal canal that presented as cauda equina syndrome involving 4 months of bilateral sciatica, paraparesis, urinary and fecal retention. The diagnosis of paraganglioma was confirmed by immunohistochemical positivity for chromogranin after microsurgical resection of the tumor.
Resumo
Paragangliomas da cauda equina são tumores de incidência rara, com ~ 220 casos descritos na literatura mundial. São lesões benignas, grau 1 pela Organização Mundial da Saúde (OMS), cujo diagnóstico definitivo apenas pode ser feito pela análise imunohistoquímica, onde se evidencia a natureza neuroendócrina dada especialmente pela presença de cromogranina. O presente relato de caso se torna importante porque este deve ser considerado entre os diagnósticos diferenciais de tumores intradurais e extramedulares, e porque há trabalhos na literatura descrevendo crises hipertensivas durante a ressecção da lesão devidas a descarga adrenérgica.
O presente estudo apresenta o caso de um paciente masculino de 36 anos diagnosticado com tumor na coluna lombar localizado no canal medular, que cursou com síndrome de cauda equina, com 4 meses de lombociatalgia bilateral, evoluindo à paraparesia, retenção urinária e fecal. Após microcirurgia para ressecção tumoral, o diagnóstico de paraganglioma só foi confirmado através da imunohistoquímica, com positividade para cromogranina.
Publication History
Received: 12 May 2020
Accepted: 09 March 2021
Article published online:
06 January 2022
© 2022. Sociedade Brasileira de Neurocirurgia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
-
References
- 1 Ardon H, Plets C, Sciot R, Calenbergh FV. Paraganglioma of the cauda equina region: A report of three cases. Surg Neurol Int 2011; 2: 96-99
- 2 Miliaras GC, Kyritsis AP, Polyzoidis KS. Cauda equina paraganglioma: a review. J Neurooncol 2003; 65 (02) 177-190
- 3 Miller CA, Torack RM. Secretory ependymoma of the filum terminale. Acta Neuropathol 1970; 15 (03) 240-250
- 4 Kliewer KE, Cochran AJ. A review of the histology, ultrastructure, immunohistology, and molecular biology of extra-adrenal paragangliomas. Arch Pathol Lab Med 1989; 113 (11) 1209-1218
- 5 Gelabert-González M. Paragangliomas of the lumbar region. Report of two cases and review of the literature. J Neurosurg Spine 2005; 2 (03) 354-365
- 6 Levy RA. Paraganglioma of the filum terminale: MR findings. AJR Am J Roentgenol 1993; 160 (04) 851-852
- 7 Corinaldesi R, Novegno F, Giovenali P, Lunardi T, Floris R, Lunardi P. Paraganglioma of the cauda equina region. Spine J 2015; 15 (03) e1-e8
- 8 Sonneland PRL, Scheithauer BW, LeChago J, Crawford BG, Onofrio BM. Paraganglioma of the cauda equina region. Clinicopathologic study of 31 cases with special reference to immunocytology and ultrastructure. Cancer 1986; 58 (08) 1720-1735
- 9 Horoupian DS, Kerson LA, Sainotz H, Valsamis M. Paraganglioma of cauda equina. Clinicopathologic and ultrastructural studies of an unusual case. Cancer 1974; 33 (05) 1337-1348
- 10 Park DH, Park YK, Oh JI. et al. Oncocytic paraganglioma of the cauda equina in a child. Case report and review of the literature. Pediatr Neurosurg 2002; 36 (05) 260-265
- 11 Araki Y, Ishida T, Ootani M. et al. MRI of paraganglioma of the cauda equina. Neuroradiology 1993; 35 (03) 232-233
- 12 Masuoka J, Brandner S, Paulus W. et al. Germline SDHD mutation in paraganglioma of the spinal cord. Oncogene 2001; 20 (36) 5084-5086
- 13 Wolansky LJ, Stewart VA, Pramanik BK. et al. Giant paraganglioma of the cauda equina in adolescence: magnetic resonance imaging demonstration. J Neuroimaging 1996; 6 (01) 54-56
- 14 Taxy JB. Paraganglioma of the cauda equina. Report of a rare tumor. Cancer 1983; 51 (10) 1904-1906
- 15 Lagacé R, Delage C, Gagné F. Paraganglioma of the filum terminale. Can J Neurol Sci 1978; 5 (02) 257-260
- 16 Yang C, Li G, Fang J. et al. Clinical characteristics and surgical outcomes of primary spinal paragangliomas. J Neurooncol 2015; 122 (03) 539-547
- 17 Iliya AR, Davis RP, Seidman RJ. Paraganglioma of the cauda equina: case report with magnetic resonance imaging description. Surg Neurol 1991; 35 (05) 366-367